Medical Device Manufacturer · LI , Triesen

Bemer Int AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2017

Recent clearances: B.Light Clear Evo and B.Light Restore Evo, Bemer Therapy System Evo, BEMER Therapy Systems, BEMER Classic Set, BEMER Pro-Set

4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Bemer Int AG General & Plastic Surgery

1 devices
1-1 of 1
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